Reacción #42730

ord-20446c10caf4475b83f552e064cafc91

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe organic phase was decanted into a separatory funnel
  2. 2
    LavadoThe organic phase was washed with brine
  3. 3
    Secadodried over Na2SO4
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated under reduced pressure

Procedimiento

To 5-bromo-2-hydroxybenzyl alcohol (93 g, 0.46 mol, available from Sigma-Aldrich) in 2.0 L of 2,2-dimethoxypropane was added 700 mL of acetone, followed by zinc chloride (170 g). After stirring for 18 hours, 1.0 M aqueous sodium hydroxide was added until the aqueous phase was basic. Diethyl ether (1.5 L) was added to the slurry and the organic phase was decanted into a separatory funnel. The organic phase was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give the title compound as an oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732441B2uspto-grants-2010_06